8-(p-iodophenyl)octyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside

Base Information

Chemical Name:8-(p-iodophenyl)octyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside
CAS No.:1357000-59-9
Molecular Formula:C₅₂H₇₂INO₂₅
Molecular Weight:1238.04
Hs Code.:

8-(p-iodophenyl)octyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside

Synonyms:8-(p-iodophenyl)octyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside

Suppliers and Price of 8-(p-iodophenyl)octyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 8-(p-iodophenyl)octyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 8-(p-iodophenyl)octyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside

There total 11 articles about 8-(p-iodophenyl)octyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 82.0%

: 1357000-57-7
8-(p-iodophenyl)octyl 2,3,4-tri-O-acetyl-β-D-glucopyranoside

: 1357000-53-3
p-octyloxyphenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-1-thio-α-D-mannopyranoside

: 1357000-59-9
8-(p-iodophenyl)octyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside

Guidance literature:: With N-iodo-succinimide; trifluorormethanesulfonic acid; In dichloromethane; at -50 ℃; for 2.5h; Molecular sieve;
DOI:10.3987/COM-11-12332

Reference yield:

: 1357000-55-5
8-(p-iodophenyl)octyl 2,3,4-tri-O-acetyl-6-O-allyloxycarbonyl-β-D-glucopyranoside

: 1357000-59-9
8-(p-iodophenyl)octyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; formic acid; triphenylphosphine / tetrahydrofuran / 1 h

2: N-iodo-succinimide; trifluorormethanesulfonic acid / dichloromethane / 2.5 h / -50 °C / Molecular sieve

With N-iodo-succinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; formic acid; trifluorormethanesulfonic acid; triphenylphosphine; In tetrahydrofuran; dichloromethane;
DOI:10.3987/COM-11-12332

Reference yield:

: 1242660-03-2
3,4,6-tri-O-acetyl-2-N-phthaloyl-β(1-2)-D-glucosaminyl-3-O-benzyl-(4,6)-benzylidene-β-D-mannopyranosyl p-octyloxyphenyl sulfoxide

: 1357000-59-9
8-(p-iodophenyl)octyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 7 steps

1: triphenylphosphine / tetrachloromethane; acetonitrile / 2 h / Reflux

2: hydrazine hydrate / ethanol; water; toluene / 5 h / Reflux

3: pyridine / 5 h

4: acetic acid / tetrahydrofuran; water / 5 h / 55 °C

5: chloro-trimethyl-silane; lithium iodide / chloroform / 6 h / 0 - 20 °C

6: pyridine; dmap / 2 h / 0 - 20 °C

7: N-iodo-succinimide; trifluorormethanesulfonic acid / dichloromethane / 2.5 h / -50 °C / Molecular sieve

With pyridine; dmap; N-iodo-succinimide; chloro-trimethyl-silane; trifluorormethanesulfonic acid; hydrazine hydrate; acetic acid; triphenylphosphine; lithium iodide; In tetrahydrofuran; tetrachloromethane; ethanol; dichloromethane; chloroform; water; toluene; acetonitrile;
DOI:10.3987/COM-11-12332